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DisGeNET
DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
| Source | Last Updated |
|---|---|
| DisGeNET | July 29, 2024 |
| Disease ID | Disease Name | Gene Symbol ▲ | Gene ID | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C0080174 | Spina Bifida Occulta | COLEC11 | 78989 | collectin subfamily member 11 | Q9BWP8 |
| C0243026 | Sepsis | COLEC11 | 78989 | collectin subfamily member 11 | Q9BWP8 |
| C0019693 | HIV Infections | COLEC11 | 78989 | collectin subfamily member 11 | Q9BWP8 |
| C3714636 | Pneumonitis | COLEC11 | 78989 | collectin subfamily member 11 | Q9BWP8 |
| C1836230 | HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO | COLEC11 | 78989 | collectin subfamily member 11 | Q9BWP8 |
| C0010278 | Craniosynostosis | COLEC11 | 78989 | collectin subfamily member 11 | Q9BWP8 |
| C0013170 | Drug habituation | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0026769 | Multiple Sclerosis | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0013146 | Drug abuse | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0524620 | Metabolic Syndrome X | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0740858 | Substance abuse problem | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0038580 | Substance Dependence | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0026848 | Myopathy | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0038586 | Substance Use Disorders | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0003850 | Arteriosclerosis | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0013222 | Drug Use Disorders | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0235946 | Cerebral atrophy | COLGALT1 | 79709 | collagen beta(1-O)galactosyltransferase 1 | Q8NBJ5 |
| C0029463 | Osteosarcoma | COLGALT1 | 79709 | collagen beta(1-O)galactosyltransferase 1 | Q8NBJ5 |
| C0027404 | Narcolepsy | COLGALT1 | 79709 | collagen beta(1-O)galactosyltransferase 1 | Q8NBJ5 |
| C0302892 | Congenital porencephaly | COLGALT1 | 79709 | collagen beta(1-O)galactosyltransferase 1 | Q8NBJ5 |
| C4082173 | Porencephaly | COLGALT1 | 79709 | collagen beta(1-O)galactosyltransferase 1 | Q8NBJ5 |
| C0036572 | Seizures | COLGALT1 | 79709 | collagen beta(1-O)galactosyltransferase 1 | Q8NBJ5 |
| C0585442 | Osteosarcoma of bone | COLGALT1 | 79709 | collagen beta(1-O)galactosyltransferase 1 | Q8NBJ5 |
| C0796154 | SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1 | COLGALT1 | 79709 | collagen beta(1-O)galactosyltransferase 1 | Q8NBJ5 |
